EP3623376B1 - Sekundäre amin-, radikal- und alkoxyaminverbindung - Google Patents

Sekundäre amin-, radikal- und alkoxyaminverbindung Download PDF

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EP3623376B1
EP3623376B1 EP19160161.6A EP19160161A EP3623376B1 EP 3623376 B1 EP3623376 B1 EP 3623376B1 EP 19160161 A EP19160161 A EP 19160161A EP 3623376 B1 EP3623376 B1 EP 3623376B1
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Prior art keywords
alkyl group
radical
alkoxy
reaction
added
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French (fr)
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EP3623376A1 (de
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Meng-Wei Wang
Yu-min HAN
Chih-Hsiang Lin
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Industrial Technology Research Institute ITRI
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/655—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms
    • C07F9/6552—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms the oxygen atom being part of a six-membered ring
    • C07F9/65522—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms the oxygen atom being part of a six-membered ring condensed with carbocyclic rings or carbocyclic ring systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
    • C07F9/6571—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms
    • C07F9/657163—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms the ring phosphorus atom being bound to at least one carbon atom
    • C07F9/657172—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms the ring phosphorus atom being bound to at least one carbon atom the ring phosphorus atom and one oxygen atom being part of a (thio)phosphinic acid ester: (X = O, S)
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F293/00—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule
    • C08F293/005—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule using free radical "living" or "controlled" polymerisation, e.g. using a complexing agent
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
    • C07F9/6571—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms
    • C07F9/6574—Esters of oxyacids of phosphorus
    • C07F9/65744—Esters of oxyacids of phosphorus condensed with carbocyclic or heterocyclic rings or ring systems
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F112/00—Homopolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
    • C08F112/02—Monomers containing only one unsaturated aliphatic radical
    • C08F112/04—Monomers containing only one unsaturated aliphatic radical containing one ring
    • C08F112/06—Hydrocarbons
    • C08F112/08—Styrene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F120/00—Homopolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
    • C08F120/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F120/10—Esters
    • C08F120/12—Esters of monohydric alcohols or phenols
    • C08F120/14—Methyl esters, e.g. methyl (meth)acrylate
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F120/00—Homopolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
    • C08F120/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F120/10—Esters
    • C08F120/12—Esters of monohydric alcohols or phenols
    • C08F120/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
    • C08F120/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2/00—Processes of polymerisation
    • C08F2/38—Polymerisation using regulators, e.g. chain terminating agents, e.g. telomerisation
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2438/00—Living radical polymerisation
    • C08F2438/02—Stable Free Radical Polymerisation [SFRP]; Nitroxide Mediated Polymerisation [NMP] for, e.g. using 2,2,6,6-tetramethylpiperidine-1-oxyl [TEMPO]

Definitions

  • the technical field relates to secondary amine, radical formed from the secondary amine, and alkoxy amine compound formed from the radical.
  • the major conventional method of forming block copolymers is controlled/living radical polymerization (CRP), which includes nitroxide mediated polymerization (NMP), atom transfer radical polymerization (ATRP), or reversible addition fragmentation chain transfer (RAFT).
  • CRP controlled/living radical polymerization
  • NMP nitroxide mediated polymerization
  • ATRP atom transfer radical polymerization
  • RAFT reversible addition fragmentation chain transfer
  • the requirements for the NMP condition are lower than those for the ATRP condition, meaning that the NMP is more feasible.
  • the NMP initiator is free of sulfur atoms, and the color of the NMP product is lighter than the color of the RAFT product.
  • nitroxide initiator (the critical technology of NMP) is usually synthesized in several steps. Accordingly, a simplified method of synthesizing a novel nitroxide for NMP is called for.
  • CN 105 254 866 A discloses a carboxyl-terminated phosphorus-containing copolyester which is formed by randomly connecting and combining specific structural units shown as I, II and III according to carboxyl and hydroxyl functional groups, and the Mw of the carboxyl-terminated phosphorus-containing copolyester is 1. 1 ⁇ 10 3 -1.3 ⁇ 10 4 g.mol -1 .
  • This document further discloses a preparation method of the carboxyl-terminated phosphorus-containing copolyester, a halogen-free flame retardant biology-based pressure sensitive adhesive composed of the carboxyl-terminated phosphorus-containing copolyester and an application.
  • One embodiment of the disclosure provides a secondary amine, having a chemical structure of: ; wherein each of R 1 is independently H, C 1-6 alkyl group, or C 1-6 alkoxy group; R 2 is C 1-6 alkyl group; and R 3 is -(C x H 2x )-OH or - (C x H 2x+1 ), and x is 1 to 8.
  • One embodiment of the disclosure provides a radical, having a chemical structure of: ; wherein each of R 1 is independently H, C 1-6 alkyl group, or C 1-6 alkoxy group; R 2 is C 1-6 alkyl group; and R 3 is -(C x H 2x )-OH or -(C x H 2x+1 ), and x is 1 to 8.
  • R 1 is independently H, C 1-6 alkyl group, or C 1-6 alkoxy group
  • R 2 is C 1-6 alkyl group
  • R 3 is -(C x H 2x )-OH or -(C x H 2x+1 ), and x is 1 to 8
  • R 4 is H or C 1-6 alkyl group
  • R 5 is and R 6 is H or C 1-8 alkyl group
  • R 7 is H or C 1-6 alkyl group
  • R 8 Ini is a residual group of a radical initiator
  • n is an integer of 1 to 10000.
  • One embodiment of the disclosure provides a secondary amine and a method of forming the same.
  • a primary amine and an aldehyde can react with each other at room temperature to form an intermediate, which can further react with a derivative of DOPO (9,10-dihydro-9-oxa-10-phosphaphenanthrene 10-oxide) at room temperature to form the secondary amine.
  • DOPO 9,10-dihydro-9-oxa-10-phosphaphenanthrene 10-oxide
  • each of R 1 is independently H, C 1-6 alkyl group, or C 1-6 alkoxy group.
  • R 2 is C 1-6 alkyl group.
  • R 3 is -(C x H 2x )-OH or -(C x H 2x+1 ), and x is 1 to 8.
  • R 2 is C 2-4 alkyl group.
  • x is 2 to 5.
  • each R 1 is H, R 2 is isopropyl group (e.g. the aldehyde is isobutyraldehyde), and R 3 is hydroxyethyl group (e.g. the primary amine is ethanolamine) or butyl group (e.g. the primary amine is butyl amine).
  • the above reaction may form the secondary amine compound of high purity at room temperature without additional purification (e.g. column chromatography), thereby dramatically lowering the manufacturing cost.
  • the secondary amine can be further oxidized to form a radical, which has a chemical structure of .
  • each of R 1 is independently H, C 1-6 alkyl group, or C 1-6 alkoxy group
  • R 2 is C 1-6 alkyl group
  • R 3 is -(C x H 2x )-OH or -(C x H 2x+1 ), and x is 1 to 8.
  • R 2 is C 2-4 alkyl group.
  • x is 2 to 5.
  • each R 1 is H, R 2 is is isopropyl group, and R 3 is hydroxyethyl group or butyl group.
  • the secondary amine can be oxidized by an oxidant such as hydrogen peroxide, peracetic acid, pertrifluoroacetic acid, nitric acid, oxone, the like, or a combination thereof to form the radical.
  • the radical may stably exist, and can collocate with another radical initiator (e.g. azobisisobutyronitrile (AIBN) or benzoyl peroxide (BPO)) to perform a NMP reaction of monomer having a double bond.
  • AIBN azobisisobutyronitrile
  • BPO benzoyl peroxide
  • R 1 is independently H, C 1-6 alkyl group, or C 1-6 alkoxy group
  • R 2 is C 1-6 alkyl group
  • R 3 is -(C x H 2x )-OH or -(C x H 2x+1 ), and x is 1 to 8
  • R 4 is H or C 1-6 alkyl group
  • R 5 is and R 6 is H or C 1-8 alkyl group
  • R 7 is H or C 1-6 alkyl group
  • R 8 is Ini is a residual group of a radical initiator
  • n is an integer of 1 to 10000.
  • R 2 is C 2-4 alkyl group.
  • x is 2 to 5.
  • each R 1 is H, R 2 is isopropyl group, and R 3 is hydroxyethyl group or butyl group.
  • the radical initiator may include AIBN or BPO.
  • AIBN, the described radical, and monomer having a double bond can be heated and reacted under nitrogen to form the alkoxy amine compound, and the heating temperature is determined by the monomer having a double bond.
  • the heating temperature can be about 60°C.
  • the heating temperature can be about 80 °C.
  • the heating temperature can be about 110°C.
  • R 4 , R 5 , R 7 , and R 8 are determined by the monomer having a double bond. For example, when the monomer having a double bond is butyl acrylate, R 4 will be H, R 5 will be and R 6 will be butyl group. When the monomer having a double bond is styrene, R 7 will be H, R 8 will be . When the monomer having a double bond is methyl methacrylate, R 4 will be methyl group, R 5 will be and R 6 will be methyl group.
  • the heating temperature is lower and the polymerization period is shorter for the radical in the disclosure, and the alkoxy amine compound of the disclosure has a higher number average molecular weight (Mn).
  • Mn number average molecular weight
  • reaction of forming the alkoxy amine compound can be any reaction of forming the alkoxy amine compound.
  • the reaction of forming the alkoxy amine compound can be
  • Ini is a residual group of a radical initiator, which is determined by the radical initiator type.
  • a radical initiator which is determined by the radical initiator type.
  • One skilled in the art should understand that the above reaction is only illustrative and not intended to limit the disclosure.
  • One skilled in the art may select suitable reagents and reactions (not limited to the above reagents and reactions) to form the described secondary amine, radical, and alkoxy amine compound.
  • Dimethylacetamide (DMAc) serving as solvent was added to the reaction bottle for preparing solution (50wt%).
  • the solution was bubbled with nitrogen to deoxygenate for 30 minutes, and then heated to 60°C and stirred to be reacted for about 2.5 hours.
  • DMAc serving as solvent was added to the reaction bottle for preparing solution (50wt%).
  • the solution was bubbled with nitrogen to deoxygenate for 30 minutes, and then heated to 60°C and stirred to be reacted for about 1 hour.
  • NMP reagents TIPNO and TIPNO • commercially available from Sigma-Aldrich
  • DMAc serving as solvent was added to the reaction bottle for preparing solution (50wt%).
  • the solution was bubbled with nitrogen to deoxygenate for 30 minutes, and then heated to 75°C and stirred to be reacted for about 16 hours.
  • the reaction result was analyzed by GPC to prove that no new reaction occurred.
  • DMAc serving as solvent was added to the reaction bottle for preparing solution (50wt%).
  • the solution was bubbled with nitrogen to deoxygenate for 30 minutes, and then heated to 125°C and stirred to be reacted for about 24 hours.
  • Example 2 As shown in the comparison between Example 1, Example 2, and Comparative Example 2, Mn of the polymers formed at a lower temperature during shorter periods in Examples 1 and 2 were dramatically larger than Mn of the polymer formed at a higher temperature during a longer period in Comparative Example 2.
  • DMAc serving as solvent was added to the reaction bottle for preparing solution (50wt%).
  • the solution was bubbled with nitrogen to deoxygenate for 30 minutes, and then heated to 80°C and stirred to be reacted for about 16 hours.
  • Example 4 As shown in the comparison between Example 3, Example 4, and Comparative Example 3, Mn of the polymers formed during shorter periods in Examples 3 and 4 were dramatically larger than Mn of the polymer formed during a longer period in Comparative Example 3.
  • DMAc serving as solvent was added to the reaction bottle for preparing solution (50wt%).
  • the solution was bubbled with nitrogen to deoxygenate for 30 minutes, and then heated to 110°C and stirred to be reacted for about 1 hour.
  • DMAc serving as solvent was added to the reaction bottle for preparing solution (50wt%).
  • the solution was bubbled with nitrogen to deoxygenate for 30 minutes, and then heated to 75°C and stirred to be reacted for about 12 hours.
  • the reaction result was analyzed by GPC to prove that no new reaction was occurred.
  • DMAc serving as solvent was added to the reaction bottle for preparing solution (50wt%).
  • the solution was bubbled with nitrogen to deoxygenate for 30 minutes, and then heated to 125°C and stirred to be reacted for about 24 hours.
  • Example 5 As shown in the comparison between Example 5 and Comparative Example 5, Mn of the polymer formed at a lower temperature during a shorter period in Example 5 was dramatically larger than Mn of the polymer formed at a higher temperature during a longer period in Comparative Example 5.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Claims (10)

  1. Sekundäres Am in mit der chemischen Struktur:
    Figure imgb0033
     wobei jede der Komponenten R1 unabhängig H, eine C1-6-Alkylgruppe oder eine C1-6-Alkoxygruppe ist,
    R2 eine C1-6-Alkylgruppeist, und
    R3 -(CxH2x)-OH oder -(CxH2x+1) ist, und x 1 bis 8 beträgt.
  2. Sekundäres Am in nach Anspruch 1, wobei R2 eine C2-4-Alkylgruppe ist.
  3. Sekundäres Am in nach Anspruch 1 oder 2, wobei x 2 bis 5 beträgt.
  4. Radikal mit der chemischen Struktur:
    Figure imgb0034
     wobei jede der Komponenten R1 unabhängig H, eine C1-6-Alkylgruppe oder eine C1-6-Alkoxygruppe ist,
    R2 eine C1-6-Alkylgruppeist, und
    R3 -(CxH2x)-OH oder -(CxH2x+1) ist, und x 1 bis 8 beträgt.
  5. Radikal nach Anspruch 4, wobei R2 eine C2-4-Alkylgruppe ist.
  6. Radikal nach Anspruch 4 oder 5, wobei x 2 bis 5 beträgt.
  7. Alkoxyaminverbindung mit der chemischen Struktur:
    Figure imgb0035
     wobei jede der Komponenten R1 unabhängig voneinander H, eine C1-6-Alkylgruppe oder eine C1-6-Alkoxygruppe ist,
    R2 eine C1-6-Alkylgruppe ist,
    R3 -(CxH2x)-OH oder -(CxH2x+1) ist, und x 1 bis 8 beträgt,
    R4 H oder eine C1-6-Alkylgruppe ist,
    R5
    Figure imgb0036
     ist, und R6 H oder eine C1-8-Alkylgruppe ist,
    R7 H oder eine C1-6-Alkylgruppe ist,
    R8
    Figure imgb0037
     ist, Ini eine Restgruppe eines Radikalinitiators ist, und
    n eine ganze Zahl von 1 bis 10000 ist.
  8. Alkoxyaminverbindung nach Anspruch 7, wobei R2 eine C2-4-Alkylgruppe ist.
  9. Alkoxyaminverbindung nach Anspruch 7 oder 8, wobei x 2 bis 5 beträgt.
  10. Alkoxyaminverbindung nach einem der Ansprüche 7 bis 9, wobei der Radikalinitiator Azobisisobutyronitril oder Benzoylperoxid aufweist.
EP19160161.6A 2018-09-11 2019-02-28 Sekundäre amin-, radikal- und alkoxyaminverbindung Active EP3623376B1 (de)

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US201862729658P 2018-09-11 2018-09-11
TW107137351A TWI701256B (zh) 2018-09-11 2018-10-23 自由基與烷氧胺化合物

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CN112645983B (zh) * 2020-12-19 2023-02-24 中国民用航空飞行学院 一种添加型可交联阻燃剂及其制备方法

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FR2788270B1 (fr) 1999-01-08 2001-03-16 Atochem Elf Sa Procede de preparation de radicaux nitroxyde beta-phosphores
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